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PV 中间神经元输出突触的抑制性 LTP 需要发育性 BMP 信号。

LTP of inhibition at PV interneuron output synapses requires developmental BMP signaling.

机构信息

Laboratory of Synaptic Mechanisms, Brain Mind Institute, School of Life Science, École Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.

Institute of Neuroscience, University of Oregon, Eugene, OR, 97403, USA.

出版信息

Sci Rep. 2020 Jun 22;10(1):10047. doi: 10.1038/s41598-020-66862-5.

DOI:10.1038/s41598-020-66862-5
PMID:32572071
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7308402/
Abstract

Parvalbumin (PV)-expressing interneurons (PV-INs) mediate well-timed inhibition of cortical principal neurons, and plasticity of these interneurons is involved in map remodeling of primary sensory cortices during critical periods of development. To assess whether bone morphogenetic protein (BMP) signaling contributes to the developmental acquisition of the synapse- and plasticity properties of PV-INs, we investigated conditional/conventional double KO mice of BMP-receptor 1a (BMPR1a; targeted to PV-INs) and 1b (BMPR1a/1b (c)DKO mice). We report that spike-timing dependent LTP at the synapse between PV-INs and principal neurons of layer 4 in the auditory cortex was absent, concomitant with a decreased paired-pulse ratio (PPR). On the other hand, baseline synaptic transmission at this connection, and action potential (AP) firing rates of PV-INs were unchanged. To explore possible gene expression targets of BMP signaling, we measured the mRNA levels of the BDNF receptor TrkB and of P/Q-type Ca channel α-subunits, but did not detect expression changes of the corresponding genes in PV-INs of BMPR1a/1b (c)DKO mice. Our study suggests that BMP-signaling in PV-INs during and shortly after the critical period is necessary for the expression of LTP at PV-IN output synapses, involving gene expression programs that need to be addressed in future work.

摘要

钙结合蛋白(PV)表达中间神经元(PV-INs)介导皮质主要神经元的适时抑制,这些中间神经元的可塑性参与了发育关键期初级感觉皮层图重构。为了评估骨形态发生蛋白(BMP)信号是否有助于 PV-INs 的突触和可塑性特性的发育获得,我们研究了 BMP 受体 1a(BMPR1a;靶向 PV-INs)和 1b(BMPR1a/1b(c)双敲除(DKO)小鼠的条件/常规双敲除。我们报告说,在听觉皮层第 4 层 PV-INs 和主神经元之间的突触上,依赖于尖峰时间的长时程增强(LTP)缺失,同时伴随着成对脉冲比(PPR)降低。另一方面,这种连接的基础突触传递和 PV-INs 的动作电位(AP)放电率保持不变。为了探索 BMP 信号的可能基因表达靶标,我们测量了 BDNF 受体 TrkB 和 P/Q 型钙通道 α 亚基的 mRNA 水平,但未检测到 BMPR1a/1b(c)DKO 小鼠中 PV-INs 相应基因的表达变化。我们的研究表明,发育关键期内和之后不久,PV-INs 中的 BMP 信号对于 PV-IN 输出突触的 LTP 表达是必需的,涉及到未来工作中需要解决的基因表达程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f6b/7308402/c003f2dc1c28/41598_2020_66862_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f6b/7308402/2d647a1e8921/41598_2020_66862_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f6b/7308402/a8306110d871/41598_2020_66862_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f6b/7308402/8ef6f762b329/41598_2020_66862_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f6b/7308402/c003f2dc1c28/41598_2020_66862_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f6b/7308402/2d647a1e8921/41598_2020_66862_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f6b/7308402/a8306110d871/41598_2020_66862_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f6b/7308402/8ef6f762b329/41598_2020_66862_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f6b/7308402/c003f2dc1c28/41598_2020_66862_Fig4_HTML.jpg

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本文引用的文献

1
Patterning the Vertebrate Retina with Morphogenetic Signaling Pathways.用形态发生信号通路对脊椎动物视网膜进行模式化。
Neuroscientist. 2020 Apr;26(2):185-196. doi: 10.1177/1073858419874016. Epub 2019 Sep 11.
2
Role of BMP Signaling for the Formation of Auditory Brainstem Nuclei and Large Auditory Relay Synapses.BMP 信号在听脑干核和大听神经中继突触形成中的作用。
Dev Neurobiol. 2019 Feb;79(2):155-174. doi: 10.1002/dneu.22661. Epub 2019 Jan 2.
3
Shared and distinct transcriptomic cell types across neocortical areas.不同脑区共有的和独特的转录组细胞类型。
Front Cell Dev Biol. 2022 Jul 6;10:934662. doi: 10.3389/fcell.2022.934662. eCollection 2022.
Nature. 2018 Nov;563(7729):72-78. doi: 10.1038/s41586-018-0654-5. Epub 2018 Oct 31.
4
Parvalbumin-Interneuron Output Synapses Show Spike-Timing-Dependent Plasticity that Contributes to Auditory Map Remodeling.钙结合蛋白阳性中间神经元输出突触表现出的突触可塑性具有时间依赖性,有助于听觉图谱的重塑。
Neuron. 2018 Aug 22;99(4):720-735.e6. doi: 10.1016/j.neuron.2018.07.018. Epub 2018 Aug 2.
5
Synapse Elimination Triggered by BMP4 Exocytosis and Presynaptic BMP Receptor Activation.BMP4 胞吐作用和突触前 BMP 受体激活触发的突触消除。
Cell Rep. 2018 Jan 23;22(4):919-929. doi: 10.1016/j.celrep.2017.12.101. Epub 2018 Jan 28.
6
Single-cell analysis of experience-dependent transcriptomic states in the mouse visual cortex.小鼠视觉皮层中经验依赖的转录组状态的单细胞分析。
Nat Neurosci. 2018 Jan;21(1):120-129. doi: 10.1038/s41593-017-0029-5. Epub 2017 Dec 11.
7
Reconstruction and Simulation of Neocortical Microcircuitry.重建与模拟新皮层微电路
Cell. 2015 Oct 8;163(2):456-92. doi: 10.1016/j.cell.2015.09.029.
8
Functional effects of distinct innervation styles of pyramidal cells by fast spiking cortical interneurons.快速发放型皮层中间神经元对锥体细胞不同支配方式的功能影响。
Elife. 2015 Jul 4;4:e07919. doi: 10.7554/eLife.07919.
9
Inhibitory and excitatory spike-timing-dependent plasticity in the auditory cortex.听觉皮层中抑制性和兴奋性的峰时依赖可塑性
Neuron. 2015 Apr 22;86(2):514-28. doi: 10.1016/j.neuron.2015.03.014. Epub 2015 Apr 2.
10
Brain structure. Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq.脑结构。单细胞 RNA 测序揭示的小鼠皮层和海马中的细胞类型。
Science. 2015 Mar 6;347(6226):1138-42. doi: 10.1126/science.aaa1934. Epub 2015 Feb 19.